3,4,5,4'-四甲氧基二苯乙烯

3,4,5,4'-四甲氧基二苯乙烯

中文名称3,4,5,4'-四甲氧基二苯乙烯
中文同义词3,4,5,4'-四甲氧基二苯乙烯;化合物DMU-212;(E)-3,4,5,4'-四甲氧基苯乙烯;(E)-3,4,5,4'-四甲氧基二苯乙烯;3,4,5,4'-四甲氧基二苯乙烯
英文名称3,4,5,4'-TETRAMETHOXYSTILBENE
英文同义词3,4,5,4'-TETRAMETHOXYSTILBENE;(E)-1,2,3-Trimethoxy-5-[2-(4-methoxyphenyl)ethenyl]benzene;DMU 212;(E)-3,4,5,4′-Tetramethoxystilbene;1,2,3-Trimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]-benzene;DMU-212;DMU 212;DMU212;Benzene, 1,2,3-trimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]-;(E)-3,4,5,4'-Tetramethoxystilbene >=98% (HPLC)
CAS号134029-62-2
分子式C18H20O4
分子量300.349
EINECS号1312995-182-4
相关类别
Mol文件134029-62-2.mol
结构式3,4,5,4'-四甲氧基二苯乙烯 结构式

3,4,5,4'-四甲氧基二苯乙烯 性质

熔点157-159℃
沸点444.0±40.0 °C(Predicted)
密度1.117
储存条件2-8°C
溶解度DMSO:可溶5mg/mL,澄清(加热)
形态粉末
颜色白色至米色

3,4,5,4'-四甲氧基二苯乙烯 用途与合成方法

DMU-212 是一种白藜芦醇 (HY-16561) 甲基化衍生物,具有抗分裂、抗增殖、抗氧化和促进细胞凋亡的活性。DMU-212 通过诱导凋亡 (apoptosis) 和激活 ERK1/2 蛋白导致有丝分裂停止。DMU-212 具有口服活性。

DMU-212 (0.3125-40 μM) inhibits growth of A375, MeWo, Bro and M5 cells human melanoma cells.
DMU-212 (30-50 μM; 24 hours) induces upregulation of cell cycle inhibitors, apoptosis and ERK activation in A375 cells.
DMU-212 induces upregulation of cell cycle inhibitors, apoptosis and ERK activation in A375 cells.
DMU-212 induces G2/M arrest and apoptosis in cancer cells.
DMU-212 induces mitotic arrest, apoptosis and activation of ERK1/2 protein.

Cell Proliferation Assay

Cell Line: A375 cells, MeWo cells, M5 cells, Bro cells
Concentration: 0.3125 μM, 0,625 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM, 20 μM, 40 μM
Incubation Time: 96 hours
Result: Inhibited the cellular proliferation of human melanoma cells at submicromolar or micromolar concentrations (IC 50 =0.5 μM for A375 and Bro and IC 50 = 1.25 μM for MeWo and M5 cells).

Cell Cycle Analysis

Cell Line: A375 cells
Concentration: 20 μM, 30 μM, 50 μM
Incubation Time: 24 hours
Result: Caused a marked increase in the levels of p21, p53 and cyclin B1 proteins with a concomitant decrease in the levels of cyclin A2.

Western Blot Analysis

Cell Line: A375 cells
Concentration: 20 μM, 30 μM, 50 μM
Incubation Time: 24 hours
Result: Significant upregulation of Bax, caspase 3 and caspase 9 protein levels, while the levels of the anti-apoptotic protein Bcl-2 were decreased.

DMU-212 (50 mg/kg; i.g.; three times a week; for 14 days) inhibits tumor growth in xenograft model of human ovarian cancer.

Animal Model: 6-weeks-old SCID female mice (20-24 g), with ovarian cancer xenografts
Dosage: 50 mg/kg
Administration: Oral gavage, three times a week, for 14 days
Result: Lower tumor burden.

安全信息

WGK Germany3

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/08/19HY-137977DMU-2121 mg248元
2024/08/19HY-1379773,4,5,4'-四甲氧基二苯乙烯
DMU-212
134029-62-210mM * 1mLin DMSO550元

3,4,5,4'-四甲氧基二苯乙烯 上下游产品信息

"3,4,5,4'-四甲氧基二苯乙烯"相关产品信息
4-硝基苯乙烯
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